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Heart Failure clinical trials

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NCT ID: NCT04529577 Recruiting - Clinical trials for Heart Failure, Systolic

His-bundle Pacing vs. Right Ventricular Apical Pacing in Patients With Reduced Ejection Fraction

HIS-PrEF
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The study compares standard right ventricle apical pacing with so called His-bundle pacing, for patients with slightly or moderately reduced ejection fraction and atrioventricular block requiring pacemaker therapy. The primary outcome is left ventricular ejection fraction measured after 6 months.

NCT ID: NCT04528004 Recruiting - Clinical trials for Heart Failure, Systolic

Mechanistic Studies of Nicotinamide Riboside in Human Heart Failure

NRII
Start date: September 26, 2020
Phase: Early Phase 1
Study type: Interventional

Preliminary animal studies by ourselves and others suggest that the dietary supplement, nicotinamide riboside (NR), may improve cardiac function in heart failure (HF) by increasing cellular levels of its metabolite, nicotinamide adenine dinucleotide (NAD+, NADH). This Study will address a key gap in current knowledge by assessing the mechanisms through which raising blood and myocardial NAD+ levels in humans mediates changes in mitochondrial function, protein and epigenetic modifications, as well as inflammation. Human myocardium will be obtained after 4-14 days of oral NR supplementation from advanced heart failure patients undergoing elective left ventricular assist device (LVAD) implantation. Positive results would provide evidence to proceed with further studies of NR as a mitochondria-targeted metabolic therapy in heart failure.

NCT ID: NCT04522609 Recruiting - Sarcopenia Clinical Trials

Electrostimulation of Skeletal Muscles in Patients Listed for a Heart Transplant

Start date: September 2020
Phase: N/A
Study type: Interventional

Heart transplantation is the best way to treat terminal heart failure, which can improve the quality and life expectancy of patients, as well as contribute to their social and labor rehabilitation. Actually, the procedure of heart transplantation is a complex procedure that requires the coordinated work of cardiologists, cardiac surgeons, anesthetists, perfusionist, nurses, as well as the administration of medical organizations. It is known that the restriction of motor activity in patients with heart failure leads to a loss of muscle mass, as well as a decrease in its strength and endurance. In patients with heart failure, the low functional status of skeletal muscle is associated with poor prognosis, regardless of gender, age, and concomitant coronary heart disease. Optimization of drug therapy and appropriate use of resynchronization therapy can improve functional status, as can patient engagement in exercise. Although exercise is recommended as a component of heart failure management, adherence is consistently low. This is particularly troubling because exercise has great potential as a low-risk, low-cost intervention to improve functional status and quality of life while decreasing heart failure symptoms and hospitalizations in patients with heart failure. Low adherence is due in part to inadequate strength and inability to tolerate or sustain even low levels of activity. In this study, we propose to use neuromuscular electrical stimulation to assist patient initiation of quadriceps strengthening in order to progressively increase low exercise tolerance.

NCT ID: NCT04522596 Recruiting - Heart Failure Clinical Trials

Effect of Dual Bronchodilation With Umeclidinium/Vilanterol on Patients With COPD, Hyperinflation and Heart Failure

CHHEF
Start date: May 21, 2021
Phase: Phase 4
Study type: Interventional

Double-blind, randomized, two-period crossover, placebo-controlled, single-center study, to determine the effect of umeclidinium/vilanterol 55/22 μg compared with placebo on the increase in left systolic chamber function during exercise in patients with COPD, lung hyperinflation and mild to moderate left ventricular dysfunction.

NCT ID: NCT04515537 Recruiting - Clinical trials for Congestive Heart Failure Chronic

Cyanophyta Aphanizomenon Flos-aquae, and Adipose Stroma Vascular Fraction, in Heart Failure Patient

Start date: May 20, 2021
Phase:
Study type: Observational

This study is a prospective, randomized, controlled trial to assess the efficacy of transplantation of autologous stroma vauscultar fraction and/or AFA in 15 patients with ischemic heart failure

NCT ID: NCT04508920 Recruiting - Heart Failure Clinical Trials

A Survey to Assess Effects of Covid-19 on Cardiovascular Patients

Start date: May 15, 2019
Phase:
Study type: Observational [Patient Registry]

The design included 152 patients with confirmed heart failure (HF) evaluated in two different periods of time: a baseline before the outbreak, and other during the outbreak of which 76 patients were randomized in each group. A care and follow-up guide was used as an instrument through a face-to-face survey (baseline group) and telemedicine (group outbreak). The primary outcome was the comparison of functional class modification observed in patients

NCT ID: NCT04506606 Recruiting - Clinical trials for Heart Failure With Preserved Ejection Fraction

Cardiac Rehab Effects in HFpEF

Start date: May 2, 2022
Phase: N/A
Study type: Interventional

This research in Veterans with heart failure with preserved ejection fraction (HFpEF) will provide new information on the mechanisms determining the patients' exercise intolerance and the efficacy of regular physical activity to improve this shortcoming by alleviating the patients' neurocirculatory abnormalities. Specifically, the investigators will focus on the role of nerves originating in working limb muscles in determining the patients' exercise intolerance and compromised fatigue resistance before and after a chronic exercise intervention. By focusing on a specific mechanism, this project will evaluate the validity of exercise as an alternative treatment strategy with the overall purpose of improving the quality of life of Veterans with HFpEF.

NCT ID: NCT04504188 Recruiting - Heart Failure Clinical Trials

Optimizing Beta Blocker Dosage in Women While Using the Wearable Cardioverter Defibrillator

OPT-BB WOMEN
Start date: March 8, 2021
Phase: N/A
Study type: Interventional

The primary objective of this pilot study is to document the percentage achievement in effective HR control (average nighttime HR < 70 bpm) during WCD use in a cohort of female patients with cardiomyopathy in an outpatient setting using continuous heart rate (HR) trends data from the WCD to optimize BB/ivabradine dosage, as compared to a prior historical control.

NCT ID: NCT04502563 Recruiting - Heart Failure Clinical Trials

LINK-HF2 - Remote Monitoring Analytics in Heart Failure

LINK-HF2
Start date: April 19, 2021
Phase: N/A
Study type: Interventional

Heart failure (HF) is a type of heart disease that leads to need of admissions to the hospital during worsening of symptoms. These admissions are expensive and very inconvenient for patients. The investigators have previously shown that monitoring of patients with a using a small wearable sensor combined with a mathematical model can detect worsening of HF before the patient needs medical care. In this study the investigators will test whether the remote monitoring and prediction of HF worsening can be used to find out when patients are at risk, change their treatment and avoid a hospitalization. The study will enroll 240 Veterans with HF and randomly assign half of them to monitoring and communication of the information on HF worsening to their medical teams. The investigators hope to find our how to best use this approach in routine care of HF. The investigators also plan to determine if this approach will indeed led to less admissions to the hospital among these patients, shorter hospital stays and better quality of life.

NCT ID: NCT04502316 Recruiting - Heart Failure Clinical Trials

Real-World Experience - Barostim™ Advancing the Level of Clinical Evidence (REBALANCE Registry)

Start date: June 26, 2020
Phase:
Study type: Observational

The purpose of this registry is to develop valid scientific evidence of the safety and benefit of Barostim Therapy in the commercial setting in patients with heart failure with reduced ejection fraction (HFrEF) that were recently implanted with the Barostim System.